TY - JOUR
T1 - Ultramicroporous carbons with extremely narrow pore size distribution via in-situ ionic activation for efficient gas-mixture separation
AU - Zhang, Peixin
AU - Wang, Jun
AU - Fan, Wei
AU - Zhong, Yao
AU - Zhang, Yan
AU - Deng, Qiang
AU - Zeng, Zheling
AU - Deng, Shuguang
N1 - Funding Information:
The research work was supported by the National Natural Science Foundation of China (No. 51672186). The authors would like to acknowledge the start-up fund from Nanchang University and Arizona State University. We show great gratitude to Arizona State University provided the raw cactus.
Funding Information:
The research work was supported by the National Natural Science Foundation of China (No. 51672186 ). The authors would like to acknowledge the start-up fund from Nanchang University and Arizona State University . We show great gratitude to Arizona State University provided the raw cactus.
PY - 2019/11/1
Y1 - 2019/11/1
N2 - Developing highly selective, cycle reliable, and moisture resistant adsorbents is of great importance for gas separation. It is very challenging to control and optimize pore sizes within the ultramicroporous ranges (<0.7 nm), especially for biomass-derived carbons. Moreover, porous carbons featured with random micropore sizes usually exhibited inferior gas separation performances. Herein, we developed an in-situ ionic activation method, in which the chemically bonded K+ ions that are uniformly distributed in the carbon precursor are able to create ultramicroporous carbons with uniform and narrow pore size distributions. Thus, the obtained carbons exhibited high CO2 uptakes (4.17 mmol g−1) and selectivities (333.2 and 34.9) for CO2/N2 (15v/85v) and CO2/CH4 (40v/60v) separation at ambient conditions. The dynamic breakthrough experiments clearly demonstrate their superior and applicable gas-mixture separation performances. Upon the detailed evaluation of vacuum swing adsorption (VSA) working parameters, a record-high adsorbent selective parameter (S) of 1906.4 is obtained. Hence, the in-situ ionic activation approach is an effective method for preparing ultramicroporous carbons with narrow and uniform pore size distributions.
AB - Developing highly selective, cycle reliable, and moisture resistant adsorbents is of great importance for gas separation. It is very challenging to control and optimize pore sizes within the ultramicroporous ranges (<0.7 nm), especially for biomass-derived carbons. Moreover, porous carbons featured with random micropore sizes usually exhibited inferior gas separation performances. Herein, we developed an in-situ ionic activation method, in which the chemically bonded K+ ions that are uniformly distributed in the carbon precursor are able to create ultramicroporous carbons with uniform and narrow pore size distributions. Thus, the obtained carbons exhibited high CO2 uptakes (4.17 mmol g−1) and selectivities (333.2 and 34.9) for CO2/N2 (15v/85v) and CO2/CH4 (40v/60v) separation at ambient conditions. The dynamic breakthrough experiments clearly demonstrate their superior and applicable gas-mixture separation performances. Upon the detailed evaluation of vacuum swing adsorption (VSA) working parameters, a record-high adsorbent selective parameter (S) of 1906.4 is obtained. Hence, the in-situ ionic activation approach is an effective method for preparing ultramicroporous carbons with narrow and uniform pore size distributions.
KW - CO capture
KW - CO/CH/N separation
KW - In-situ
KW - Ionic activation
KW - Narrow pore distribution
KW - Ultramicroporous carbon
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U2 - 10.1016/j.cej.2019.121931
DO - 10.1016/j.cej.2019.121931
M3 - Article
AN - SCOPUS:85067839688
SN - 1385-8947
VL - 375
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 121931
ER -